Branched blocky cationic organopolysiloxane

ABSTRACT

Disclosed herein are inventive branched blocky cationic organopolysiloxanes and consumer product compositions comprising such organopolysiloxanes. Such compositions can deposit effectively onto target substrates to deliver consumer-desired benefits such as conditioning, anti-wrinkle, softness, and anti-static.

FIELD OF THE INVENTION

The present invention relates to inventive branched blocky cationic organopolysiloxane compounds. It also relates to consumer product compositions comprising the inventive compounds and to methods of making and use.

BACKGROUND OF THE INVENTION

Cationic conditioning polymers meant for deposition onto negatively charged surfaces, such as fabric, skin, or hair, are included in many common consumer product compositions. Such products can provide consumer-desired benefits such as softness, lubricity, hand, anti-wrinkle, hair conditioning, frizz control, skin moisturization, and color protection. The effectiveness of any particular conditioning polymer depends not only upon the chemical and physical properties of the conditioning polymer itself, but also upon those of the targeted surface and the product formulation in which the conditioning polymer is delivered.

Many consumer products containing cationic conditioning polymers are in the form of aqueous-based rinse-off compositions, such as hair shampoos, body washes, laundry detergents, and fabric softeners. Despite the popularity of these rinse-off compositions, such product forms frequently experience difficulties effectively depositing these cationic conditioning polymers, which are typically hydrophobic, onto the target surfaces. Incorporating these conditioners into aqueous-based products often results in the conditioner being preferentially rinsed away from the intended site of deposition, rather than effectively deposited. This problem is particularly pronounced in the context of cleansing compositions containing surfactant, especially those containing anionic surfactant.

Anionic surfactants can interfere with deposition by forming complexes/precipitates with the cationic conditioning polymers. The higher the concentration of anionic surfactant, the more difficult it becomes to deposit cationic benefit actives. This leads to non-cost-effective use and waste of materials. Further, even if an acceptable level of deposition is attained, these formulations may lack shelf-stability due to flocculation and precipitation, making them unacceptable as consumer products.

Several materials exist in the art, but are not wholly satisfactory. For example, the material described by Ono (WO 99/32539) comprises functionalized end groups having heteroatoms such as oxygen, nitrogen, sulfur, or halogens. These functionalized end groups can lead to undesirable reactions that pose stability issues for compositions comprising these materials. For instance, Ono's silicones can react further through these end groups, leading to further condensation and/or polymerization of the silicones in the compositions during storage.

Also known in the art are quaternized silicones that include alkylene oxide units, such as those described by Masschelein (U.S. Pat. No. 6,903,061). The quaternized silicones described by Masschelein may be too water soluble for a given application, and thus can have a reduced capacity as conditioning polymers, since these materials tend to partition into water at a higher than desired level rather than deposit on the target substrate. Further, when these materials are used as the conditioning active, they can have an undesirable feel because of their high permeability to water and water vapor. Additionally, because of the potential for variability in the alkylene oxide moiety, these materials can be difficult to formulate reproducibly. This can limit the desired degree of functionality in a silicone material. It would desirable to have a material the provides greater flexibility via the level of quaternization. Similarly, the ethoxylated quaternized silicone materials disclosed by Boutique (U.S. Pat. No. 6,833,344) suffer from many of the same inadequacies of those described by Masschelein.

There is still a need to provide cationic conditioning polymers that are suitable for use in a wide range of consumer product applications. The present invention provides cationic conditioning polymers and consumer product compositions comprising conditioning polymers that can effectively deposit and provide conditioning benefits to negatively charged substrates while avoiding the aforementioned disadvantages.

SUMMARY OF THE INVENTION

The present invention attempts to solve one or more of the aforementioned needs by providing, in one aspect, inventive branched blocky cationic organopolysiloxanes that are suitable for use in a wide range of consumer product compositions. The inventive compounds are functionalized to favorably interact with the targeted substrate and product composition to deliver desired deposition and conditioning benefits, as well as desired shelf-stability.

Without being bound by theory, when cationic charge that could otherwise facilitate hydrophobic benefit agent deposition is randomly distributed along the length of the benefit agent polymer, the charge can be too highly dispersed to adequately facilitate deposition. The inventive polymer's charge density can be custom-tailored (e.g., higher charge density) to enhance deposition and conditioning performance in different use environments. Further, by varying the inventive polymer's level of hydrophobic substitution and/or the degree of ethoxylation, propoxylation, and alkoxylation, the inventive polymer can be formulated into a desirably stable composition for a variety of use environments. By controlling charge density and hydrophobic substitution and/or degree of ethoxylation, propoxylation, and more generally alkoxylation, the inventive compounds can be custom-tailored for a variety of product formulations and uses.

The current invention further solves the aforementioned needs by providing branching in the cationic portion of the cationic organopolysiloxane polymer. Without being bound by theory it is felt that the branching in the cationic portion of the cationic organopolysiloxane provides for a further increase in the charge density of the cationic portions thereby increasing the deposition efficiency of the cationic organopolysiloxane.

DETAILED DESCRIPTION OF THE INVENTION I. Definitions

As used herein, the “branched blocky cationic organopolysiloxane” may also be referred to as the “organopolysiloxane”.

As used herein “consumer product” means baby care, personal care, fabric & home care, family care (e.g., facial tissues, paper towels), feminine care, health care, beauty care and like products generally intended to be used or consumed in the form in which they are sold. Such products include but are not limited to diapers, bibs, and wipes; products for and/or methods relating to treating hair (human, dog, and/or cat), including, bleaching, coloring, dyeing, conditioning, shampooing, styling; deodorants and antiperspirants; personal cleansing; cosmetics; skin care including application of creams, lotions, and other topically applied products for consumer use including fine fragrances; and shaving products, products for and/or methods relating to treating fabrics, hard surfaces and any other surfaces in the area of fabric and home care, including: air care including air fresheners and scent delivery systems, car care, dishwashing, fabric conditioning (including softening and/or freshening), laundry detergency, laundry and rinse additive and/or care, hard surface cleaning and/or treatment including floor and toilet bowl cleaners, and other cleaning for consumer or institutional use; products and/or methods relating to bath tissue, facial tissue, paper handkerchiefs, and/or paper towels; tampons, feminine napkins; products and/or methods relating to oral care including toothpastes, tooth gels, tooth rinses, denture adhesives, and tooth whitening.

As used herein, the term “cleansing and/or treatment composition” is a subset of consumer products that includes, unless otherwise indicated, personal care, fabric care, and home care products. Such products include, but are not limited to, products for treating hair (human, dog, and/or cat), including, bleaching, coloring, dyeing, conditioning, shampooing, styling; deodorants and antiperspirants; personal cleansing; cosmetics; skin care including application of creams, lotions, and other topically applied products for consumer use including fine fragrances; and shaving products, products for treating fabrics, hard surfaces and any other surfaces in the area of fabric and home care, including: air care including air fresheners and scent delivery systems, car care, dishwashing, fabric conditioning (including softening and/or freshening), laundry detergency, laundry and rinse additive and/or care, hard surface cleaning and/or treatment including floor and toilet bowl cleaners, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, including antibacterial hand-wash types, cleaning bars, mouthwashes, denture cleaners, dentifrice, car or carpet shampoos, bathroom cleaners including toilet bowl cleaners; hair shampoos and hair-rinses; shower gels, fine fragrances and foam baths and metal cleaners; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets, dry and wetted wipes and pads, nonwoven substrates, and sponges; as well as sprays and mists all for consumer or/and institutional use; and/or methods relating to oral care including toothpastes, tooth gels, tooth rinses, denture adhesives, tooth whitening. The care agents can advantageously be used in household polishes and cleaners for floors and countertops to provide benefits such as enhanced shine. Care agents in fabric softeners can help preserve “newness” because of their softening properties, and those having elasticity can help smooth out wrinkles. The care agents can also enhance shoe cleaning and polishing products.

As used herein, the term “personal care cleansing and/or treatment composition” is a subset of cleaning and treatment compositions that includes, unless otherwise indicated, products for treating hair, including, bleaching, coloring, dyeing, conditioning, shampooing, styling; deodorants and antiperspirants; personal cleansing; cosmetics; skin care including application of creams, lotions, and other topically applied products for consumer use including fine fragrances; and shaving products; liquid cleaning and disinfecting agents including antibacterial hand-wash types, cleaning bars, mouthwashes, denture cleaners, and dentifrice cleaners; hair shampoos and hair-rinses; shower gels, fine fragrances, and foam baths; substrate-laden products such as dry and wetted wipes and pads, nonwoven substrates, and sponges; as well as sprays and mists all for consumer or/and institutional use; and/or methods relating to oral care including toothpastes, tooth gels, tooth rinses, denture adhesives, and tooth whitening.

As used herein, the term “fabric and/or hard surface cleansing and/or treatment composition” is a subset of cleaning and treatment compositions that includes, unless otherwise indicated, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, including antibacterial hand-wash types, cleaning bars, car or carpet shampoos, bathroom cleaners including toilet bowl cleaners; and metal cleaners, fabric conditioning products including softening and/or freshening that may be in liquid, solid and/or dryer sheet form; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets, dry and wetted wipes and pads, nonwoven substrates, and sponges; as well as sprays and mists. All of such products, as applicable, may be in standard, concentrated or even highly concentrated form even to the extent that such products may in certain aspects be non-aqueous.

As used herein, articles such as “a” and “an” are understood to mean one or more of what is claimed or described.

As used herein, the terms “include”, “contain”, and “have” are non-limiting and do not exclude other components or features beyond those expressly identified in the description or claims.

As used herein, the terms “treatment agent”, “benefit agent”, “active”, “active agent”, and/or “care agent” and the like are used interchangeably to mean materials that can impart desirable aesthetic and/or functional properties (e.g., conditioning benefits such as softening or freshening) to a substrate. For example, the inventive organopolysiloxane polymer of the present invention can be used as a conditioning agent to impart conditioning benefits to substrates.

As used herein, the terms “conditioning agent” and “conditioning aid” are used interchangeably to refer to a material that delivers desirable conditioning effects (e.g., benefits such as softening or freshening) to a substrate. Conditioning agents are a type of treatment agent.

As used herein, the term “conditioning polymer” means a polymer that delivers desirable conditioning effects (e.g., softening or freshening) to a substrate.

As used herein, the term “substrate” is synonymous and used interchangeably with the terms “situs” and “surface”. Non-limiting examples of substrates include paper products, fabrics, garments, hard surfaces, hair, and skin.

As used herein, “targeted substrate” means a substrate, or the relevant portion of a substrate, upon which deposition is intended.

As used herein, a “deposition aid” is a material that assists another material (e.g., a benefit agent) to deposit (e.g., adhere) to a targeted substrate. The term “deposition aid” is broad enough to encompass both polymeric deposition aids (i.e. “deposition polymer”) and non-polymeric deposition aids.

As used herein, “adjunct” means an optional material that can be added to a composition to complement the aesthetic and/or functional properties of the composition.

As used herein, “auxiliary composition” refers to one or more compositions that when combined with a benefit agent emulsion of the present invention, form a consumer product composition. The auxiliary composition may be in the form of one or more ingredients or ingredient combinations.

As used herein, “carrier” means an optional material, including but not limited to a solid or fluid, that can be combined with a benefit agent (e.g., conditioning polymers) to facilitate delivery and/or use of the benefit agent.

As used herein, the term “solid” includes granular, powder, bar and tablet product forms.

As used herein, the term “fluid” includes liquid, gel, paste and gas product forms including unitized-dose forms that generally include a fluid composition enclosed in a pouch or other delivery vehicle.

As used herein, the term “particle” includes solid and semi-solid particles, as well as emulsion droplets.

Unless otherwise indicated, all percentages and ratios herein are calculated based on weight.

All percentages and ratios are calculated based on weight of the total composition unless otherwise indicated.

Unless specified otherwise, all molecular weights are given in Daltons.

Unless otherwise indicated, all molecular weights are weight average molecular weights as determined by size exclusion chromatography using a MALS detector (SEC-MALS), as is commonly known by those skilled in the art. A MALS detector (Multi-Angle Light Scattering Detector, such as those manufactured by Malvern Instruments Ltd., Malvern, UK) determines absolute molecular weight, rather than relative molecular weight (i.e., determined relative to a standard).

Unless otherwise noted, all component (i.e., ingredient) or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.

The term “charge density”, as used herein, refers to the ratio of the number of positive charges on a monomeric unit of which a polymer is comprised, to the molecular weight of said monomeric unit. The charge density multiplied by the polymer molecular weight determines the number of positively charged sites on a given polymer chain. The charge density calculation can also be expressed as:

${{charge}\mspace{14mu}{density}}\mspace{14mu} = {\frac{\left( {{moles}\mspace{14mu}{of}\mspace{14mu} N} \right)\left( {{charge}\mspace{14mu}{per}\mspace{14mu} N} \right)}{\left( {{moles}\mspace{14mu}{of}\mspace{14mu}{polymer}} \right)\left( {{molecular}\mspace{14mu}{weight}\mspace{14mu}{of}\mspace{14mu}{the}\mspace{14mu}{polymer}} \right)} \times 100}$

As used herein, the term “hydrocarbon polymer radical” means a polymeric radical comprising only carbon and hydrogen.

As used herein, “ethylene moiety” means a divalent CH₂CH₂ moiety.

As used herein, the term “siloxyl residue” means a polydialkylsiloxane moiety.

As used herein, the nomenclature SiO_(n/2) represents the ratio of oxygen and silicon atoms. For example, SiO_(1/2) means that, on average, one oxygen atom is shared between two silicon atoms. Likewise SiO_(2/2) means that, on average, two oxygen atoms are shared between two silicon atoms and SiO_(3/2) means that, on average, three oxygen atoms are shared between two silicon atoms.

As used herein, the terms “substantially no”, “substantially free of”, and/or “substantially free from” mean that the indicated material is at the very minimum not deliberately added to the composition to form part of it, or, preferably, is not present at analytically detectable levels. It is meant to include compositions whereby the indicated material is present only as an impurity in one of the other materials deliberately included.

It should be understood that every maximum numerical limitation given throughout this specification includes every lower numerical limitation, as if such lower numerical limitations were expressly written herein. Every minimum numerical limitation given throughout this specification will include every higher numerical limitation, as if such higher numerical limitations were expressly written herein. Every numerical range given throughout this specification will include every narrower numerical range that falls within such broader numerical range, as if such narrower numerical ranges were all expressly written herein.

II. Branched Blocky Cationic Organopolysiloxane Polymers

The present invention provides a branched blocky cationic organopolysiloxane having the formula: M_(w)D_(x)T_(y)Q_(z) wherein:

-   -   M is selected from the group consisting of [SiR₁R₂R₃O_(1/2)],         [SiR₁R₂G₁O_(1/2)], [SiR₁G₁G₂O_(1/2)], [SiG₁G₂G₃O_(1/2)], and         combinations thereof;     -   D is selected from the group consisting of [SiR₁R₂O_(2/2)],         [SiR₁G₁O_(2/2)], [SiG₁G₂O_(2/2)], and combinations thereof;     -   T is selected from the group consisting of [SiR₁O_(3/2)],         [SiG₁O_(3/2)], and combinations thereof;         Q=[SiO_(4/2)];     -   w is an integer from 1 to about (2+y+2z);     -   x is an integer from about 5 to about 15,000;     -   y is an integer from 0 to about 98;     -   z is an integer from 0 to about 98;     -   R₁, R₂ and R₃ are each independently selected from the group         consisting of H, OH, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl,         C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂         alkylaryl, C₆-C₃₂ substituted alkylaryl, C₁-C₃₂ alkoxy, C₁-C₃₂         substituted alkoxy, C₁-C₃₂ alkylamino, and C₁-C₃₂ substituted         alkylamino;     -   and wherein at least one of M, D, and T incorporates at least         one moiety G₁, G₂ or G₃ and G₁, G₂, and G₃ are same or different         moieties each of which has the formula:

-   -   wherein:         -   N is a nitrogen atom;         -   Each R₄ is independently selected from the group consisting             of H,

-   -   -    C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂             aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl,             and C₆-C₃₂ substituted alkylaryl;         -   Each X comprises a divalent radical selected from the group             consisting of C₁-C₃₂ alkylene, C₁-C₃₂ substituted alkylene,             optionally interrupted with a hetero atom selected from the             group consisting of P, N and O, C₅-C₃₂ or C₆-C₃₂ arylene,             C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene,             C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkyleneamino,             C₁-C₃₂ substituted alkyleneamino, ring-opened epoxide and             ring-opened glycidyl;         -   Each E comprises the same or different divalent radicals             selected from the group consisting of C₁-C₃₂ alkylene,             C₁-C₃₂ substituted alkylene, alkylene, optionally             interrupted with a hetero atom selected from the group             consisting of P, N and O, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂             or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂             substituted arylalkylene, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted             alkoxy, C₁-C₃₂ alkyleneamino, C₁-C₃₂ substituted             alkyleneamino, ring-opened epoxide and ring-opened glycidyl;         -   Each R₅ is independently selected from the group consisting             of H, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or             C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂             alkylaryl, and C₆-C₃₂ substituted alkylaryl;         -   With the proviso that at least one Nitrogen-atom within at             least one moiety G₁, G₂ or G₃ has at least 2 R₄ selected to             be

-   -   And wherein:     -   Each m is an integer independently selected from 2 to 100,     -   Each n is an integer independently selected from 1 or 2,     -   And when an organopolysiloxane portion of a moiety G₁, G₂, G₃ is         positively charged, A^(−t) is a suitable charge balancing anion         or anions such that the total charge of all occurrences of the         charge-balancing anion or anions, A^(−t) and kA^(−t), is equal         to and opposite from the net charge on the organopolysiloxane         portions of the moiety G₁, G₂ or G₃.         -   It would be appreciated by one of ordinary skill in the art             that:         -   A is an anionic counter ion to the positively charge             organopolysiloxane,         -   t is the charge on any individual counter ion, and         -   k is the coefficient of any such counterion             so that the net charge of the positively charge             organopolysiloxane and the sum total of the counter ions is             neutral.

In one aspect, the counter ion or ions A^(−t) is selected from the group consisting of Cl—, Br—, I—, methylsulfate, toluene sulfonate, carboxylate, phosphate, hydroxide, acetate, formate, carbonate, nitrate, and combinations thereof.

-   -   In one aspect of the present invention, the at least one         Nitrogen-atom within at least one moiety G₁, G₂ or G₃ that has         at least 2 R₄ selected to be

is adjacent a moiety X.

-   -   In one aspect of the present invention, the at least one         Nitrogen-atom within at least one moiety G₁, G₂ or G₃ that has         at least 2 R₄ selected to be

is adjacent a moiety E. In one embodiment, the branched blocky cationic organopolysiloxane has the formula: M_(w)D_(x)T_(y)Q_(z)

-   -   M is [SiR₁R₂G₁O_(1/2)],     -   D is [SiR₁R₂O_(2/2)],     -   w is 2,     -   x is an integer from about 40 to about 1000,     -   y and z are each 0,     -   R₁, R₂ and are independently selected from the group consisting         of H, OH, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or         C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂         alkylaryl, C₆-C₃₂ substituted alkylaryl, C₁-C₃₂ alkoxy, C₁-C₃₂         substituted alkoxy,     -   G₁ has the formula:

-   -   wherein:         -   Each X comprises a divalent radical selected from the group             consisting of C₁-C₃₂ alkylene, C₁-C₃₂ substituted alkylene,             optionally interrupted with a hetero atom selected from the             group consisting of P, N and O, C₅-C₃₂ or C₆-C₃₂ arylene,             C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene,             C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkyleneamino,             C₁-C₃₂ substituted alkyleneamino, ring-opened epoxide and             ring-opened glycidyl;         -   N is a nitrogen atom;         -   Each R₄ is independently selected from the group consisting             of H,

-   -   -    C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂             aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl,             and C₆-C₃₂ substituted alkylaryl;         -   Each E comprises the same or different divalent radicals             selected from the group consisting of C₁-C₃₂ alkylene,             C₁-C₃₂ substituted alkylene, alkylene, optionally             interrupted with a hetero atom selected from the group             consisting of P, N and O, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂             or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂             substituted arylalkylene, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted             alkoxy, C₁-C₃₂ alkyleneamino, C₁-C₃₂ substituted             alkyleneamino, ring-opened epoxide and ring-opened glycidyl;         -   Each R₅ is independently selected from the group consisting             of H, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or             C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂             alkylaryl, and C₆-C₃₂ substituted alkylaryl;         -   With the proviso that at least one Nitrogen-atom within at             least one moiety G₁, G₂ or G₃ has at least 2 R₄ selected to             be

-   -   And wherein:     -   Each m is an integer independently selected from 2 to 100,     -   Each n is an integer independently selected from 1 or 2,     -   And when an organopolysiloxane portion of a moiety G₁, G₂, G₃ is         positively charged, A^(−t) is a suitable charge balancing anion         or anions such that the total charge of all occurrences of the         charge-balancing anion or anions, A^(−t) and kA^(−t), is equal         to and opposite from the net charge on the organopolysiloxane         portions of the moiety G₁, G₂ or G₃         -   It would be appreciated by one of ordinary skill in the art             that:         -   A is an anionic counter ion to the positively charge             organopolysiloxane,         -   t is the charge on any individual counter ion, and         -   k is the coefficient of any such counterion             so that the net charge of the positively charge             organopolysiloxane and the sum total of the counter ions is             neutral.             In one embodiment, the branched blocky cationic             organopolysiloxane has the formula:             M_(w)D_(x)T_(y)Q_(z)     -   M is [SiR₁R₂O₁O_(1/2)],     -   D is [SiR₁R₂O_(2/2)],     -   W is 2,     -   x is an integer from about 40 to about 1000,     -   y and z are each 0,     -   R₁, R₂ and are each, independently, selected from the group         consisting of H, OH, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl,         C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂         alkylaryl, C₆-C₃₂ substituted alkylaryl, C₁-C₃₂ alkoxy, C₁-C₃₂         substituted alkoxy, G₁ has the formula:

-   -   wherein         Each R₄ is independently selected from the group consisting of         H,

C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl; wherein:

-   -   X comprises a divalent radical selected from the group         consisting of C₁-C₃₂ alkylene, C₁-C₃₂ substituted alkylene,         optionally interrupted with a hetero atom selected from the         group consisting of P, N and O, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂         or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂         substituted arylalkylene, C₁-C₃₂ alkyleneamino, C₁-C₃₂         substituted alkyleneamino, ring-opened epoxide and ring-opened         glycidyl;     -   N is a nitrogen atom;     -   R₅ is selected from the group consisting of H, C₁-C₃₂ alkyl,         C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or         C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂         substituted alkylaryl optionally interrupted with a hetero atom         selected from the group consisting of P, N and O, C₁-C₃₂ alkoxy,         C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkyleneamino, C₁-C₃₂         substituted alkyleneamino;     -   Each E comprises same or different divalent radicals selected         from the group consisting of C₁-C₃₂ alkylene, C₁-C₃₂ substituted         alkylene, alkylene, optionally interrupted with a hetero atom         selected from the group consisting of P, N and O, C₅-C₃₂ or         C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂         arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkoxy,         C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkyleneamino, C₁-C₃₂         substituted alkyleneamino, ring-opened epoxide and ring-opened         glycidyl;     -   With the proviso that at least one Nitrogen-atom within at least         one moiety G₁, G₂ or G₃ has at least 2 R₄ selected to be

-   -   And wherein:     -   Each m is an integer independently selected from 2 to 100,     -   Each n is an integer independently selected from 1 or 2,     -   And when an organopolysiloxane portion of a moiety G₁, G₂, G₃ is         positively charged, A^(−t) is a suitable charge balancing anion         or anions such that the total charge of all occurrences of the         charge-balancing anion or anions, A^(−t) and kA^(−t), is equal         to and opposite from the net charge on the organopolysiloxane         portions of the moiety G₁, G₂ or G₃.         -   It would be appreciated by one of ordinary skill in the art             that:         -   A is an anionic counter ion to the positively charge             organopolysiloxane,         -   t is the charge on any individual counter ion, and         -   k is the coefficient of any such counterion     -   so that the net charge of the positively charge         organopolysiloxane and the sum total of the counter ions is         neutral.

III. Methods of Making the Branched Blocky Cationic Organopolysiloxane

Embodiments of the present invention can be made as follows. An amount of functional silicone is added to a clean vessel under inert atmosphere. The functional silicone may be an amino functional silicone or a silicone with an organic group capable of reacting with an amino function, examples of organic groups capable of reacting with an amino function include halogen functional silicones or epoxy functional silicones. Optionally, a solvent such as isopropanol or tetrahydrofuran is added. The reaction is optionally mixed and quantities of diamine and difunctional organic compounds capable of reacting with the amino functions of the amine compounds are added, either simultaneously or sequentially. For example, the difunctional organic compound capable of reacting with the amino function may be added first and the diamine added second, to obtain the desired organopolysiloxane. Alternately, these reagents may be added in reverse order.

The reaction is run at a temperature appropriate for the reagents. For example, when the difunctional organic compound capable of reacting with the amino functions is a dichloride, the reaction may be run at relatively higher temperatures (typically above 60° C. and often above 80° C.). Alternately, when the difunctional organic compound capable of reacting with the amino functions is a dibromide, the reaction may be run at relatively lower temperatures, including at room temperature (e.g., 21° C.). Alternately, when the difunctional organic compound capable of reacting with the amino functions is an activated dichloride, the reaction may be run at relatively lower temperatures, including at room temperature (e.g., 21° C.). One of ordinary skill in the art would understand the reaction conditions suitable for the specific difunctional organic compound capable of reacting with the amino functions.

The above making process is also generally described by Lange (U.S. Pat. No. 7,563,856). One skilled in the art would understand how the general process disclosed in Lange can be reapplied to the present development in order to produce the organopolysiloxanes of the present invention.

In one embodiment, the reaction is run without the addition of solvent, resulting in a substantially solvent-free process for making the organopolysiloxane of the present invention.

In another embodiment, the reaction is run and subsequently excess amine is added. Without being bound by theory, it is believed that the excess amine will consume the reactive groups of any residual difunctional organic compounds capable of reacting with the amino functions.

In another embodiment, the reaction mixture is further reacted with an amine containing molecule. Non-limiting examples of such amines include ammonia, methylamine, dimethylamine, trimethylamine, triethylamine or ethanolamine or diethanolamine. Without being bound by theory it is believed that this further reaction caps un-reacted akyl-halide functionality.

In another embodiment, the reaction mixture is further reacted with a mono-functional organic species capable of reacting with the amine functionality of the organopolysiloxane. Non-limiting examples of such mono-functional organic species include: methyl bromide, methyl iodide, and ethylbromide. Without being bound by theory it is believed that this further reaction helps to quaternize any residual neutral amine groups of the organopolysiloxane, including the terminal amine functionality.

Without being bound by theory it is expected that primary and secondary amines can react multiple times to form secondary, tertiary and quaternized amines. This can lead to branching at the amine groups. It is also thought that the reaction conditions can be modified to increase the degree of branching. Reaction conditions involving an initial excess quantity of the groups capable of reacting with an amine over the concentration of the primary or secondary amines can lead to higher levels of branching. Subsequent addition of tertiary diamines can then lead to chain growth of the branched amines.

IV. Uses of the Organopolysiloxane Compositions

The organopolysiloxanes according to the present invention can be formulated into a variety of consumer product compositions that can be applied to substrates in order to impart consumer-desired benefits, such as conditioning. Such substrates can include fabric, non-woven materials, paper products, hard surface materials, and biological materials (e.g., keratinous materials such as hair or skin).

The consumer product compositions comprising the organopolysiloxane polymers of the present invention may be prepared by any suitable process, such as processes known by those skilled in the art. For example, the organopolysiloxane polymers can be incorporated directly into the composition's other ingredients without pre-emulsification and/or pre-mixing to form the finished products. Alternatively, the organopolysiloxane may be mixed with surfactants, solvents, suitable adjuncts, and/or any other suitable ingredients to prepare emulsions prior to compounding the finished products.

The consumer product composition can comprise one or more surfactants. The surfactants may comprise cationic, anionic, non-ionic, zwitterionic, and/or amphoteric surfactants. In one embodiment, at least one surfactant is anionic. Various forms of the consumer product composition can be aqueous or non-aqueous; in one embodiment, an aqueous composition has a pH greater than 3, or greater than 5.

The composition may also comprise at least one benefit agent. Benefit agents can be hydrophobic or hydrophilic. Useful hydrophobic benefit agents include silicones, vinyl polymers, polyethers, materials comprising a hydrocarbon wax, hydrocarbon liquids, fluid sugar polyesters, fluid sugar polyethers, and mixtures thereof. In one embodiment, the silicones that are useful as benefit agents are organosilicones. In another embodiment, the silicone benefit agent is selected from the group consisting of a polydimethylsiloxane, an aminosilicone, a cationic silicone, a silicone polyether, a cyclic silicone, a silicone resin, a fluorinated silicone, and mixtures thereof. In one embodiment, the benefit agent is a liquid at room temperature. In another embodiment, the benefit agent is a solid or semi-solid at room temperature. In one embodiment, the benefit agent is a perfume or a silicone. Further, the benefit agent may be encapsulated. In one embodiment, the benefit agent is an encapsulated perfume.

The organopolysiloxane may be pre-emulsified prior to compounding into a consumer product composition. In one embodiment, a benefit agent is included with the organopolysiloxane in the pre-emulsion. In one embodiment, the benefit agent and the organopolysiloxane mixture can form a particle in the pre-emulsion.

Materials which may be helpful in creating such emulsions include: Tergitol 15-S-5, Terigtol 15-S-12, and TMN-10. The suspensions can be made by mixing the components together using a variety of mixing devices. Examples of suitable overhead mixers include: IKA Labortechnik, and Janke & Kunkel IKA WERK, equipped with impeller blade Divtech Equipment R1342. In some cases, high shear processing is required to obtain a narrow particle size distribution. Example of a suitable high shear processing device is M-110P Microfluidizer from Microfluidics.

EXAMPLES

The following examples 1-10 further describe and demonstrate exemplary embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration and are not to be construed as limitations of the present invention since many variations thereof are possible without departing from the spirit and scope of the invention. Ingredients are identified by chemical name, or otherwise defined below.

To a clean vessel is added the quantity of silicones (available from Gelest Co., Morrisville, Pa.) shown in Table 1 and an amount of isopropanol (available from Sigma-Aldrich, Milwaukee, Wis.) equal to the amount of silicone. This is mixed by stirring the sample at 30 rpm for one hour and then the quantity of dihalide (available from Sigma-Aldrich, Milwaukee, Wis.) is added and mixed by stiffing at 30 rpm for 2 hours at 50° C. After two hours, the quantity of diamine (available from Sigma-Aldrich, Milwaukee, Wis.) shown in the table is added. This is followed by heating the sample at 50° C. for 16 hours.

TABLE 1 Amino Silicone Weight (g) Molecular Weight Weight (g) Weight (g) Example # starting material¹ Silicone (Daltons) Silicone x Dihalide Dihalide Diamine 1 DMS-A15  50 g 3000 40 16.27 g Dibromo 11.47 g Hexane 2 DMS-A15  25 g 3000 40 40.67 g Dibromo 28.67 g Hexane 3 DMS-A32 250 g 30000 400 8.13  Dibromo  5.74 g Hexane 4 DMS-A32 100 g 30000 400 32.53 g Dibromo 22.93 g Hexane 5 DMS-A32 500 g 30000 400 21.87 g Dibromo 11.47 g Dodecane 6 DMS-A32 250 g 30000 400  7.20 g Dibromo  5.73 g Butane 7 DMS-A15  50 g 3000 40 41.67 g 1,4-dichloro- 28.67 g 2-butene 8 DMS-A32  50 g 30000 400  1.67 g 1,4-dichloro-  2.29 g 2-butene 9 DMS-A32  50 g 30000 400  4.17 g 1,4-dichloro-  5.73 g 2-butene 10 DMS-A32 100 g 30000 400  2.93 g p-  1.55 g dichloroxylene ¹= catalogue numbers of aminosilicone starting material, available from Gelest Company, Morrisville, PA) End-Use Formulations:

Exemplary organopolysiloxanes of the present invention are formulated into different product chassis to make various consumer product formulations. In some embodiments, the organopolysiloxane is added to the ingredient mixture in the form of an emulsion.

Emulsion Preparation:

The following emulsions are prepared for use in the consumer product formulation examples set forth herein.

The organopolysiloxanes from Examples 1-10 above are used to make the emulsions used in making the consumer product formulation examples below.

The organopolysiloxanes from Examples 1-10 are first emulsified using a homogenizer at 3,500 rpm, and then microfluidized at 20,000 psi to obtain sub-micron size emulsions (mean particle size 250 nm, as measured using Horriba instrumentation as known in the art).

TABLE 2 Material % Organopolysiloxane of Examples 1-10 20.00 Tergitol 15-S-5¹ 3.00 Acetic Acid 0.60 Dilution Water q.s. to 100% 1. ¹Available from Sigma Aldrich Hair Care Compositions Comprising the Organopolysiloxanes:

Examples below list non-limiting examples of hair care shampoo and conditioner compositions comprising emulsions of the organopolysiloxane conditioning polymers of the present invention.

Shampoos are Prepared as Follows:

Material % active in shampoo Deionized Water q.s. to 100% SLE1S ¹ 10.50% CMEA ²  0.85% Na₄EDTA  0.14% NaBenzoate  0.25% Citric acid  0.22% SLS ³  1.50% CAPB ⁴  1.00% Kathon  0.03% Emulsion according to Table 2  5.00% C500 Guar ⁵  0.25% ¹ Sodium Laureth Sulfate, 28% active, supplier: P&G ² Cocoamide MEA available as Monamid CMA, 85% active, available from Goldschmidt Chemical ³ Sodium Lauryl Sulfate, 29% active from P&G ⁴ Cocoamidopropyl Betaine available as Tego ® betaine F-B, 30% active, available from Goldschmidt Chemicals ⁵ Jaguar ® C500, MW—500,000, CD = 0.7, available from Rhodia Ingredients are combined and mixed by conventional means as known by one of ordinary skill in the art. Hair Conditioners are Prepared as Follows:

Material % active in conditioner Cetyl Alcohol 1.21% Stearyl Alcohol 3.00% Behentrimonium methosulfate/IPA ¹ 2.47% Benzyl Alcohol 0.43% Deionized Water q.s. to 100% Perfume 0.59% EDTA 0.15% Emulsions according to Table 2 5.00% ¹ Behentrimonium methosulfate/Isopropyl alcohol, available as Genamin BTMS from Clariant

Ingredients are combined and mixed by conventional means as known by one of ordinary skill in the art.

Top Sheets and Paper:

It can be appreciated by one of ordinary skill in the art that any of a number of means of applying the organopolysiloxane to the nonwoven can be utilized. The organopolysiloxane may be emulsified prior to application to the nonwoven, including emulsification into water or other primarily aqueous carrier. The organopolysiloxane may be dissolved in a suitable carrier prior to application to the nonwoven. The carrier may be volatile to facilitate removal of the carrier after treatment of the nonwoven. In one non-limiting example of the present invention, any of the organopolysiloxanes of Examples 1-10 is emulsified as described in Table 2 and air sprayed onto a 24 gsm (grams per square meter) non-woven top sheet to obtain a final coating of 5 gsm. Top sheets are air dried overnight and allowed to equilibrate in a controlled humidity room.

Fabric Care Compositions:

Examples below list non-limiting examples of Fabric Care composition comprising mulsions of the organopolysiloxane conditioning polymers of the present invention.

Heavy Duty Liquid (HDL) Laundry Detergent Formula are Prepared as Follows:

Material % in HDL HDL AE1.8S Paste ¹ 26.83 DTPA 50% ACTIVE ²  0.63 HDL Brightener 15 Premix ³  3.03 Monoethanolamine (MEA)  2.26 C₁₂/C₁₄ AMINE OXIDE ⁴  1.69 Alkoxylated polyamine HOD Base ⁵  1.20 CAUSTIC SODA (NaOH)  0.53 Anionic Detergent Blend MVP-2 Paste ⁶  4.25 Borax Premix for HDL ⁷  6.06 C11.8 HLAS ⁸  4.19 CITRIC ACID SOLUTION ⁹  5.34 C12-18 FATTY ACID ¹⁰  1.42 CALCIUM FORMATE  0.84 Water q.s. to 100% Subtilisins (NFNA-HA Base )¹¹—(54.5 mg/g)  1.27 MANNANASE (25.6 mg/g)  0.06 NATALASE (29.26 mg/g)  0.31 Polyethyleneimine Ethoxylate PE-20 (ODD-Base) ¹²  1.89 Emulsions according to Table 2 20.00 ¹ Available from Shell Chemicals, Houston, TX ² Diethylenetriaminepentaacetic acid, sodium salt ³ Available from The Procter & Gamble Company, Cincinnati, OH ⁴ Available from The Procter & Gamble Company, Cincinnati, OH ⁵ Available from BASF, AG, Ludwigshafen ⁶ Available from The Procter & Gamble Company, Cincinnati, OH ⁷ Available from Univar, Cincinnati, OH ⁸ Available from Huntsman Chemicals, Salt Lake City, UT ⁹ Available from Ciba Specialty Chemicals, High Point, NC ¹⁰ Available from Enencor International, South San Francisco, CA. ¹¹ Available from Genencor, Rochester, NY ¹² Available from BASF, AG, Ludwigshafen

Ingredients are combined and mixed by conventional means as known by one of ordinary skill in the art.

Fabric Softener Compositions are Prepared as Follows:

EXAMPLE COMPOSITION 78 Fabric Softener Active¹ 11.0 Fabric Softener Active² — Cationic Starch³ — Polyethylene imine⁴ — Quatemized polyacrylamide⁵ 0.2 Calcium chloride 0.15 Ammonium chloride 0.1 Suds Suppressor⁶ — Emulsions according to Table 2 15.0 Perfume 2.0 Perfume microcapsule⁷ 0.75 Water, suds suppressor, stabilizers, pH control agents, q.s. to 100% buffers, dyes & other optional ingredients pH = 3.0 ¹N,N di(tallowoyloxyethyl)-N,N dimethylammonium chloride available from Evonik Corporation, Hopewell, VA. ²Reaction product of fatty acid with Methyldiethanolamine, quaternized with Methylchloride, resulting in a 2.5:1 molar mixture of N,N-di(tallowoyloxyethyl) N,N-dimethylammonium chloride and N-(tallowoyloxyethyl) N-hydroxyethyl N,N-dimethylammonium chloride available from Evonik Corporation, Hopewell, VA. ³Cationic starch based on common maize starch or potato starch, containing 25% to 95% amylose and a degree of substitution of from 0.02 to 0.09, and having a viscosity measured as Water Fluidity having a value from 50 to 84. Available from National Starch, Bridgewater, NJ ⁴Available from Nippon Shokubai Company, Tokyo, Japan under the trade name Epomin 1050. ⁵Cationic polyacrylamide polymer such as a copolymer of acrylamide/[2-(acryloylamino)ethyl]tri-methylammonium chloride (quaternized dimethyl aminoethyl acrylate) available from BASF, AG, Ludwigshafen under the trade name Sedipur 544. ⁶SILFOAM ® SE90 available from Wacker AG of Munich, Germany ⁷Available from Appleton Paper of Appleton, WI

Ingredients are combined and mixed by conventional means as known by one of ordinary skill in the art.

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm.”

Every document cited herein, including any cross referenced or related patent or application and any patent application or patent to which this application claims priority or benefit thereof, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention. 

What is claimed is:
 1. A branched blocky cationic organopolysiloxane having the formula: M_(w)D_(x)T_(y)Q_(z) wherein: M is selected from the group consisting of [SiR₁R₂R₃O_(1/2)], [SiR₁R₂G₁O_(1/2)], [SiR₁G₁G₂O_(1/2)], [SiG₁G₂G₃O_(1/2)], and combinations thereof; D is selected from the group consisting of [SiR₁R₂O_(2/2)], [SiR₁G₁O_(2/2)], [SiG₁G₂O_(2/2)], and combinations thereof; T is selected from the group consisting of [SiR₁O_(3/2)], [SiG₁O_(3/2)], and combinations thereof, Q=[SiO_(4/2)]; w is an integer from 1 to about (2+y+2z); x is an integer from about 5 to about 15,000; y is an integer from 0 to about 98; z is an integer from 0 to about 98; R₁, R₂, and R₃ are each independently selected from the group consisting of H, OH, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, C₆-C₃₂ substituted alkylaryl, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkylamino, and C₁-C₃₂ substituted alkylamino; wherein at least one of M, D, and T incorporates at least one moiety G₁, G₂, or G₃ and G₁, G₂, and G₃ are same or different moieties each of which has the formula:

wherein: each X comprises a divalent radical selected from the group consisting of C₁-C₃₂ alkylene, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkyleneamino, and C₁-C₃₂ substituted alkyleneamino; N is a nitrogen atom; each R₄ is independently selected from the group consisting of H,

 C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl; each E comprises the same or different divalent radicals selected from the group consisting of C₁-C₃₂ alkylene, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkyleneamino, and C₁-C₃₂ substituted alkyleneamino; each R₅ is independently selected from the group consisting of H, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl; with the proviso that at least one Nitrogen-atom within at least one moiety G₁, G₂, or G₃ has at least 2 R₄ selected to be

wherein: each m is an integer independently selected from 2 to 100, each n is an integer independently selected from 1 or 2, and wherein when an organopolysiloxane portion of a moiety G₁, G₂, or G₃ is positively charged, A^(−t) is a suitable charge balancing anion or anions such that the total charge of all occurrences of the charge-balancing anion or anions, A^(−t) and kA^(−t), is equal to and opposite from the net charge on the organopolysiloxane portions of the moiety G₁, G₂ or G₃.
 2. A branched blocky cationic organopolysiloxane according to claim 1 wherein the at least one Nitrogen-atom within at least one moiety G₁, G₂, or G₃ that has at least 2 R₄ selected to be

is adjacent a moiety X.
 3. A branched blocky cationic organopolysiloxane according to claim 1 wherein the at least one Nitrogen-atom within at least one moiety G₁, G₂, or G₃ that has at least 2 R₄ selected to be

is adjacent a moiety E.
 4. A branched blocky cationic organopolysiloxane according to claim 1 wherein: M is [SiR₁R₂G₁O_(1/2)], D is [SiR₁R₂O_(2/2)], w is 2, x is an integer from about 40 to about 1000, y and z are each 0, R₁ and R₂ are independently selected from the group consisting of H, OH, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, C₆-C₃₂ substituted alkylaryl, C₁-C₃₂ alkoxy, and C₁-C₃₂ substituted alkoxy, G₁ has the formula:

wherein: each X comprises a divalent radical selected from the group consisting of C₁-C₃₂ alkylene, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkyleneamino, and C₁-C₃₂ substituted alkyleneamino; N is a nitrogen atom; each R₄ is independently selected from the group consisting of H,

C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl; each E comprises the same or different divalent radicals selected from the group consisting of C₁-C₃₂ alkylene, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkyleneamino, and C₁-C₃₂ substituted alkyleneamino; each R₅ is independently selected from the group consisting of H, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl; with the proviso that at least one Nitrogen-atom within at least one moiety G₁, G₂, or G₃ has at least 2 R₄ selected to be

wherein: each m is an integer independently selected from 2 to 100, each n is an integer independently selected from 1 or 2, and wherein when an organopolysiloxane portion of a moiety G₁, G₂, or G₃ is positively charged, A^(−t) is a suitable charge balancing anion or anions such that the total charge of all occurrences of the charge-balancing anion or anions, A^(−t) and kA^(−t), is equal to and opposite from the net charge on the organopolysiloxane portions of the moiety G₁, G₂, or G₃.
 5. A branched blocky cationic organopolysiloxane according to claim 2 wherein: M is [SiR₁R₂G₁O_(1/2)], D is [SiR₁R₂O_(2/2)], w is 2, x is an integer from about 40 to about 1000, y and z are each 0, R₁ and R₂ are each, independently, selected from the group consisting of H, OH, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, C₆-C₃₂ substituted alkylaryl, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted alkoxy, G₁ has the formula:

wherein each R₄ is independently selected from the group consisting of H,

C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl; wherein: each X comprises a divalent radical selected from the group consisting of C₁-C₃₂ alkylene, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkyleneamino, and C₁-C₃₂ substituted alkyleneamino; N is a nitrogen atom; each R₅ is selected from the group consisting of H, C₁-C₃₂ alkyl, C₁-C₃₂ substituted alkyl, C₅-C₃₂ or C₆-C₃₂ aryl, C₅-C₃₂ or C₆-C₃₂ substituted aryl, C₆-C₃₂ alkylaryl, and C₆-C₃₂ substituted alkylaryl optionally interrupted with a hetero atom selected from the group consisting of P, N and O, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkyleneamino, C₁-C₃₂ substituted alkyleneamino; each E comprises same or different divalent radicals selected from the group consisting of C₁-C₃₂ alkylene, C₅-C₃₂ or C₆-C₃₂ arylene, C₅-C₃₂ or C₆-C₃₂ substituted arylene, C₆-C₃₂ arylalkylene, C₆-C₃₂ substituted arylalkylene, C₁-C₃₂ alkoxy, C₁-C₃₂ substituted alkoxy, C₁-C₃₂ alkyleneamino, and C₁-C₃₂ substituted alkyleneamino; with the proviso that at least one Nitrogen-atom within at least one moiety G₁, G₂, or G₃ has at least 2 R₄ selected to be

wherein: each m is an integer independently selected from 2 to 100, each n is an integer independently selected from 1 or 2, and wherein when an organopolysiloxane portion of a moiety G₁, G₂, or G₃ is positively charged, A^(−t) is a suitable charge balancing anion or anions such that the total charge of all occurrences of the charge-balancing anion or anions, A^(−t) and kA^(−t), is equal to and opposite from the net charge on the organopolysiloxane portions of the moiety G₁, G₂, or G₃.
 6. A branched blocky cationic organopolysiloxane according to claim 1, wherein A^(−t) is selected from the group consisting of Cl—, Br—, I—, methylsulfate, toluene sulfonate, carboxylate, phosphate, hydroxide, acetate, formate, carbonate, nitrate, and combinations thereof. 